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rs13096142

From SNPedia

Orientationplus
Stabilizedplus
Make rs13096142(C;C)
Make rs13096142(C;T)
Make rs13096142(T;T)
ReferenceGRCh38 38.1/142
Chromosome3
Position46240253
is asnp
is mentioned by
dbSNPrs13096142
ebirs13096142
HLIrs13096142
Exacrs13096142
Varsomers13096142
Maprs13096142
PheGenIrs13096142
hapmaprs13096142
1000 genomesrs13096142
hgdprs13096142
ensemblrs13096142
gopubmedrs13096142
geneviewrs13096142
scholarrs13096142
googlers13096142
pharmgkbrs13096142
gwascentralrs13096142
openSNPrs13096142
23andMers13096142
23andMe allrs13096142
SNP Nexus

SNPshotrs13096142
SNPdbers13096142
MSV3drs13096142
GWAS Ctlgrs13096142
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24999842OA-icon.png]
Trait Celiac disease
Title Genome-wide association study of celiac disease in North America confirms FRMD4B as new celiac locus.
Risk Allele
P-val 4E-8
Odds Ratio 1.30 [1.18-1.43]